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Home > products > API Active Pharmaceutical Ingredient > 2-PhenylethylaMine CAS 64-04-0

2-PhenylethylaMine CAS 64-04-0

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 64-04-0

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Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Plastic bottles, Plastic buckets

Delivery Time: 7-15 days

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Supply Ability: TON

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Highlight:
CAS NO::
64-04-0
Appearance::
Colourless Or Slightly Yellow Liquid
Molecular Formula::
C8H11N
Molecular Weight::
121.18000
EINECS NO::
200-574-4
MDL NO::
MFCD00008184
CAS NO::
64-04-0
Appearance::
Colourless Or Slightly Yellow Liquid
Molecular Formula::
C8H11N
Molecular Weight::
121.18000
EINECS NO::
200-574-4
MDL NO::
MFCD00008184
2-PhenylethylaMine CAS 64-04-0

Product Description:

Product Name: 2-PhenylethylaMine CAS NO: 64-04-0

 

 

Synonyms:

1-Amino-2-phenylethane;

β-Phenylethylamine;

Phenylethylamine;

 

 

Chemical & Physical Properties:

Appearance: Colourless or slightly yellow liquid

Assay :≥99.0%

Density: 0.962

Boiling Point: 194-202℃

Melting Point: -60℃

Flash Point: 90℃

Refractive Index: 1.532-1.534

Water Solubility: SOLUBLE

Stability: Stable. Combustible. Incompatible with strong oxidizing agents, strong acids.

Storage Condition: 2-8℃

Vapor Density: 4.18 (vs air)

 

 

Safety Information:

RTECS: SG8750000

Hazard Class: 8

Safety Statements: S26-S36/37/39-S45

HS Code: 29214980

WGK Germany: 1

Packing Group: III

RIDADR: UN 2922

Risk Statements: R22; R34

Hazard Code: C

 

 

Phenethyla-mine (PEA), also known as β-phenylethylamine (β-PEA) and 2-phenylethylamine is an organic compound and a natural monoamine alkaloid, a trace amine, and also the name of a class of chemicals with many members that are well known for their psychoactive and stimulant effects.

Phenylethylamine functions as a monoaminergic neuromodulator and, to a lesser extent, a neurotransmitter in the human central nervous system. It is biosynthesized from the amino acid L-phenylalanine by enzymatic decarboxylation via the enzyme aromatic L-amino acid decarboxylase. In addition to its presence in mammals, phenethyla-mine is found in many other organisms and foods, such as chocolate, especially after microbial fermentation. It is sold as a dietary supplement for purported mood and weight loss-related therapeutic benefits; however, orally ingested phenethyla-mine experiences extensive first-pass metabolism by monoamine oxidase B (MAO-B) and then aldehyde dehydrogenase (ALDH), which metabolize it into phenylace-tic acid. This prevents significant concentrations from reaching the brain when taken in low doses.

The group of phenethyla-mine derivatives is referred to as the phenethyla-mines. Substituted phenethyla-mines, substituted amphetamines, and substituted methylenedioxyphenethyla-mines (MDxx) are a series of broad and diverse classes of compounds derived from phenethyla-mine that include empathogens, stimulants, psychedelics, anxiolytics (hypnotics) and entactogens, as well as anorectics, bronchodilators, decongestants, and antidepressants, among others.

 

 

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